SK64899A3 - Enzymatic process for the preparation of cephalosporanic 7beta-(4-carboxybutanamide) acid by means of the modified enzyme d-aminoacid oxidase of i(trigonopsis variabilis) produced in i(escherichia coli) - Google Patents
Enzymatic process for the preparation of cephalosporanic 7beta-(4-carboxybutanamide) acid by means of the modified enzyme d-aminoacid oxidase of i(trigonopsis variabilis) produced in i(escherichia coli) Download PDFInfo
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- SK64899A3 SK64899A3 SK648-99A SK64899A SK64899A3 SK 64899 A3 SK64899 A3 SK 64899A3 SK 64899 A SK64899 A SK 64899A SK 64899 A3 SK64899 A3 SK 64899A3
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- WIIZWVCIJKGZOK-RKDXNWHRSA-N chloramphenicol Chemical compound ClC(Cl)C(=O)N[C@H](CO)[C@H](O)C1=CC=C([N+]([O-])=O)C=C1 WIIZWVCIJKGZOK-RKDXNWHRSA-N 0.000 description 1
- BKHZIBWEHPHYAI-UHFFFAOYSA-N chloroform;3-methylbutan-1-ol Chemical compound ClC(Cl)Cl.CC(C)CCO BKHZIBWEHPHYAI-UHFFFAOYSA-N 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000004737 colorimetric analysis Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 101150077852 dao1 gene Proteins 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- HAXVIVNBOQIMTE-UHFFFAOYSA-L disodium;2-(carboxylatomethylamino)acetate Chemical compound [Na+].[Na+].[O-]C(=O)CNCC([O-])=O HAXVIVNBOQIMTE-UHFFFAOYSA-L 0.000 description 1
- 238000001962 electrophoresis Methods 0.000 description 1
- 239000006167 equilibration buffer Substances 0.000 description 1
- ZMMJGEGLRURXTF-UHFFFAOYSA-N ethidium bromide Chemical compound [Br-].C12=CC(N)=CC=C2C2=CC=C(N)C=C2[N+](CC)=C1C1=CC=CC=C1 ZMMJGEGLRURXTF-UHFFFAOYSA-N 0.000 description 1
- 229960005542 ethidium bromide Drugs 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 108010063718 gamma-glutamylaspartic acid Proteins 0.000 description 1
- 238000010353 genetic engineering Methods 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 108010055341 glutamyl-glutamic acid Proteins 0.000 description 1
- XBGGUPMXALFZOT-UHFFFAOYSA-N glycyl-L-tyrosine hemihydrate Natural products NCC(=O)NC(C(O)=O)CC1=CC=C(O)C=C1 XBGGUPMXALFZOT-UHFFFAOYSA-N 0.000 description 1
- 108010062266 glycyl-glycyl-argininal Proteins 0.000 description 1
- 108010023364 glycyl-histidyl-arginine Proteins 0.000 description 1
- 108010066198 glycyl-leucyl-phenylalanine Proteins 0.000 description 1
- YMAWOPBAYDPSLA-UHFFFAOYSA-N glycylglycine Chemical compound [NH3+]CC(=O)NCC([O-])=O YMAWOPBAYDPSLA-UHFFFAOYSA-N 0.000 description 1
- 108010015792 glycyllysine Proteins 0.000 description 1
- 108010087823 glycyltyrosine Proteins 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 108010028295 histidylhistidine Proteins 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- BPHPUYQFMNQIOC-NXRLNHOXSA-N isopropyl beta-D-thiogalactopyranoside Chemical compound CC(C)S[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O BPHPUYQFMNQIOC-NXRLNHOXSA-N 0.000 description 1
- 229960000318 kanamycin Drugs 0.000 description 1
- 229930027917 kanamycin Natural products 0.000 description 1
- SBUJHOSQTJFQJX-NOAMYHISSA-N kanamycin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CN)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O[C@@H]2[C@@H]([C@@H](N)[C@H](O)[C@@H](CO)O2)O)[C@H](N)C[C@@H]1N SBUJHOSQTJFQJX-NOAMYHISSA-N 0.000 description 1
- 229930182823 kanamycin A Natural products 0.000 description 1
- 108010044311 leucyl-glycyl-glycine Proteins 0.000 description 1
- 108010034529 leucyl-lysine Proteins 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 230000001320 lysogenic effect Effects 0.000 description 1
- 108010009298 lysylglutamic acid Proteins 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 229930182817 methionine Natural products 0.000 description 1
- OJURWUUOVGOHJZ-UHFFFAOYSA-N methyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-(2-methoxy-2-oxoethyl)amino]ethyl]amino]acetate Chemical compound C=1C=CC=C(OC(C)=O)C=1CN(CC(=O)OC)CCN(CC(=O)OC)CC1=CC=CC=C1OC(C)=O OJURWUUOVGOHJZ-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000002751 oligonucleotide probe Substances 0.000 description 1
- 230000002018 overexpression Effects 0.000 description 1
- 108010073025 phenylalanylphenylalanine Proteins 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000009145 protein modification Effects 0.000 description 1
- 230000033998 protein modification process Effects 0.000 description 1
- 238000001742 protein purification Methods 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 238000012163 sequencing technique Methods 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 238000002415 sodium dodecyl sulfate polyacrylamide gel electrophoresis Methods 0.000 description 1
- 238000000527 sonication Methods 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229960002180 tetracycline Drugs 0.000 description 1
- 229930101283 tetracycline Natural products 0.000 description 1
- 235000019364 tetracycline Nutrition 0.000 description 1
- 150000003522 tetracyclines Chemical class 0.000 description 1
- 108010061238 threonyl-glycine Proteins 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 108010080629 tryptophan-leucine Proteins 0.000 description 1
- 108010038745 tryptophylglycine Proteins 0.000 description 1
- 239000012138 yeast extract Substances 0.000 description 1
- 108010082737 zymolyase Proteins 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/0004—Oxidoreductases (1.)
- C12N9/0012—Oxidoreductases (1.) acting on nitrogen containing compounds as donors (1.4, 1.5, 1.6, 1.7)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/0004—Oxidoreductases (1.)
- C12N9/0012—Oxidoreductases (1.) acting on nitrogen containing compounds as donors (1.4, 1.5, 1.6, 1.7)
- C12N9/0014—Oxidoreductases (1.) acting on nitrogen containing compounds as donors (1.4, 1.5, 1.6, 1.7) acting on the CH-NH2 group of donors (1.4)
- C12N9/0022—Oxidoreductases (1.) acting on nitrogen containing compounds as donors (1.4, 1.5, 1.6, 1.7) acting on the CH-NH2 group of donors (1.4) with oxygen as acceptor (1.4.3)
- C12N9/0024—D-Amino acid oxidase (1.4.3.3)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P35/00—Preparation of compounds having a 5-thia-1-azabicyclo [4.2.0] octane ring system, e.g. cephalosporin
- C12P35/06—Cephalosporin C; Derivatives thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Genetics & Genomics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Microbiology (AREA)
- General Health & Medical Sciences (AREA)
- Biotechnology (AREA)
- Molecular Biology (AREA)
- Medicinal Chemistry (AREA)
- Biomedical Technology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Enzymes And Modification Thereof (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ES009702008A ES2131018B1 (es) | 1997-09-25 | 1997-09-25 | Un procedimiento enzimatico para preparar acido 7beta-(4-carboxibutanamido)cefalosporanico utilizando la enzima d-aminoacido oxidasa de trigonopsis variabilis modificada producida en escherichia coli. |
| PCT/ES1998/000262 WO1999015632A1 (es) | 1997-09-25 | 1998-09-24 | UN PROCEDIMIENTO ENZIMATICO PARA PREPARAR ACIDO 7β-(4-CARBOXIBUTANAMIDO) CEFALOSPORANICO UTILIZANDO LA ENZIMA D-AMINOACIDO OXIDASA DE TRIGONOPSIS VARIABILIS MODIFICADA PRODUCIDA EN ESCHERICHIA COLI. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SK64899A3 true SK64899A3 (en) | 2000-05-16 |
Family
ID=8300695
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK648-99A SK64899A3 (en) | 1997-09-25 | 1998-09-24 | Enzymatic process for the preparation of cephalosporanic 7beta-(4-carboxybutanamide) acid by means of the modified enzyme d-aminoacid oxidase of i(trigonopsis variabilis) produced in i(escherichia coli) |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US6635458B2 (cs) |
| EP (1) | EP0969088A1 (cs) |
| JP (1) | JP2001506868A (cs) |
| KR (1) | KR20000069110A (cs) |
| CN (1) | CN1246147A (cs) |
| AU (1) | AU9162898A (cs) |
| CA (1) | CA2272354A1 (cs) |
| CZ (1) | CZ182399A3 (cs) |
| EE (1) | EE9900205A (cs) |
| ES (1) | ES2131018B1 (cs) |
| HU (1) | HUP0000797A2 (cs) |
| IL (1) | IL129533A0 (cs) |
| LT (1) | LT4628B (cs) |
| LV (1) | LV12359B (cs) |
| SK (1) | SK64899A3 (cs) |
| WO (1) | WO1999015632A1 (cs) |
| ZA (1) | ZA988754B (cs) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100342014C (zh) * | 2004-04-08 | 2007-10-10 | 百瑞全球有限公司 | 重组d-氨基酸氧化酶 |
| CN1912130B (zh) * | 2005-08-08 | 2011-06-15 | 百瑞全球有限公司 | 一种用于制备7-氨基头孢霉烷酸的两步酶法 |
| CN101016540B (zh) * | 2006-02-10 | 2010-04-07 | 台湾尖端先进生技医药股份有限公司 | C-端含有组氨酸标记的hoxb4重组蛋白质的制造方法及用途 |
| RU2412998C1 (ru) * | 2009-11-18 | 2011-02-27 | Общество с ограниченной ответственностью "Инновации и высокие технологии МГУ" | Мутантная оксидаза d-аминокислот |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2268022B1 (cs) * | 1974-04-22 | 1977-06-24 | Rhone Poulenc Ind | |
| JPS62262994A (ja) * | 1986-05-12 | 1987-11-16 | Asahi Chem Ind Co Ltd | D−アミノ酸オキシダ−ゼ遺伝子 |
| CA1340522C (en) * | 1987-03-10 | 1999-05-04 | Heinz Dobeli | Fusion proteins containing neighbouring histidines for improved purification |
| CA2100987C (en) | 1992-07-27 | 1999-06-15 | Kaoru Furuya | A transformant capable of producing d-amino acid oxidase |
| US5397653A (en) | 1993-04-30 | 1995-03-14 | Westinghouse Electric Corporation | Filler wire composition and method of welding turbine component with filter wire composition and its product thereof |
| ES2109194B1 (es) | 1996-04-22 | 1998-07-16 | Antibioticos Sa | Un procedimiento para producir la enzima d-aminoacido oxidasa de rhodotorula gracilis en celulas hospedantes. |
-
1997
- 1997-09-25 ES ES009702008A patent/ES2131018B1/es not_active Expired - Fee Related
-
1998
- 1998-09-23 ZA ZA988754A patent/ZA988754B/xx unknown
- 1998-09-24 EP EP98943898A patent/EP0969088A1/en not_active Withdrawn
- 1998-09-24 JP JP51859999A patent/JP2001506868A/ja not_active Ceased
- 1998-09-24 WO PCT/ES1998/000262 patent/WO1999015632A1/es not_active Ceased
- 1998-09-24 CZ CZ991823A patent/CZ182399A3/cs unknown
- 1998-09-24 EE EEP199900205A patent/EE9900205A/xx unknown
- 1998-09-24 SK SK648-99A patent/SK64899A3/sk unknown
- 1998-09-24 KR KR1019997004579A patent/KR20000069110A/ko not_active Ceased
- 1998-09-24 AU AU91628/98A patent/AU9162898A/en not_active Abandoned
- 1998-09-24 CA CA002272354A patent/CA2272354A1/en not_active Abandoned
- 1998-09-24 CN CN98801336A patent/CN1246147A/zh active Pending
- 1998-09-24 HU HU0000797A patent/HUP0000797A2/hu unknown
- 1998-09-24 US US09/308,683 patent/US6635458B2/en not_active Expired - Fee Related
- 1998-09-24 IL IL12953398A patent/IL129533A0/xx unknown
-
1999
- 1999-05-11 LT LT99-051A patent/LT4628B/lt not_active IP Right Cessation
- 1999-05-25 LV LVP-99-87A patent/LV12359B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CN1246147A (zh) | 2000-03-01 |
| HUP0000797A2 (en) | 2000-07-28 |
| ZA988754B (en) | 1999-06-28 |
| US6635458B2 (en) | 2003-10-21 |
| WO1999015632A1 (es) | 1999-04-01 |
| LT4628B (lt) | 2000-02-25 |
| CZ182399A3 (cs) | 1999-09-15 |
| JP2001506868A (ja) | 2001-05-29 |
| ES2131018B1 (es) | 2000-04-01 |
| AU9162898A (en) | 1999-04-12 |
| EP0969088A1 (en) | 2000-01-05 |
| ES2131018A1 (es) | 1999-07-01 |
| KR20000069110A (ko) | 2000-11-25 |
| CA2272354A1 (en) | 1999-04-01 |
| IL129533A0 (en) | 2000-02-29 |
| LT99051A (en) | 1999-10-25 |
| US20030119087A1 (en) | 2003-06-26 |
| EE9900205A (et) | 1999-12-15 |
| LV12359A (lv) | 1999-10-20 |
| LV12359B (en) | 2000-03-20 |
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